HIV chemokines

ABSTRACT

Disclosed is a gene comprising an open reading frame encoded on the plus strand of the pro-viral DNA, and located in the region of HIV-1 long terminal repeat. The gene encodes a protein that is related to, and has a structural motif resembling that of chemokine proteins. Depending upon the ribosomal frameshift, a plurality of proteins may be translated from the antisense RNA. The protein has similarity with chemokine SDF-1 and may play a role as a cofactor with gp120 in the binding to and entry of HIV to a target cell.

This application claims the priority of provisional application Ser. No. 60/074,640 filed on Feb. 13, 1998, and is also a continuation-in-part of application Ser. No. 08/853,703 filed on May 9, 1997, now U.S. Pat. No. 5,919,677.

This invention was made with government support under grant IR29AI38114-01 awarded by the National Institutes of Health. The government has certain rights in the invention.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a novel gene of HIV, the virus causing AIDS, which encodes a protein having an amino acid sequence that is closely related to the chemokine family of proteins. More particularly, the invention relates to a novel HIV protein that may be a cofactor for binding to the chemokine receptor on human cells during the entry phase of infection.

2. Description of the Background and Related Art

1. The Chemokine Receptors as Coreceptor for HIV Infection

Efficient entry of HIV into target cells is dependent upon a high affinity binding of the viral envelope glycoprotein, gp120, to the amino terminal domain of CD4, a protein expressed on the surface of the target cell. While CD4 is the primary virus receptor, CD4 alone is not sufficient for virus entry. Chemokine receptors have been identified as the coreceptors involved in the entry of HIV into target cells.

Macrophage-tropic (“M-tropic”) HIV-1 use the β-chemokine receptor CCR5, and less often receptor CCR3, as their coreceptor (Choe et al., 1996, Cell 85:1135-1148; Dragic et al., 1996, Nature 381:667-673; Deng et al., 1996, Nature 381:661-666). Mutations in CCR5 appears to confer resistance to infection by M-tropic HIV-1 viruses in vivo and in vitro (Samson et al., 1996, Nature 382:722-725). T-tropic (lymphotropic strains which grow in cells including transformed T cell lines) HIV generally use the α-chemokine receptor CXCR4 (also known as fusin, SDF-1 chemokine receptor, LESTR; Feng et al., 1996, Science 272:872-877). CXCR4 also can function as the primary receptor for HIV-2 entry and infection of human CD4-negative cells (Endres et al., 1996, Cell 87:745-756). Dual-tropic primary HIV-1 isolates, that can infect both macrophages and T cells, can use either CCR5 or CXCR4 (and possibly CCR3 or CCR-2b) as the coreceptor involved in virus entry (Doranz et al., 1996, Cell 85:1149-1158). There is evidence suggesting that the structure of the gp120 V3 loop influences the ability of HIV to bind the chemokine receptors on the target cell (Choe et al., 1996, supra; Doranz et al., 1996, supra).

2. HIV Secondary Structures

Single stranded RNA form localized regions of secondary structures such as hairpin loops and pseudoknot structures (Schimm, 1989, Cell, 58-9-12). A RNA population was isolated that bound to HIV reverse transcriptase and that has a pseudoknot consensus (Tuerk et al., 1992, Proc. Natl. Acad. Sci., USA. 59:6988-6992). Pseudoknots are structures in which there is an intramolecular base pairing of the “loop” sequence of an RNA hairpin to sequences either 5′ or 3′ to that hairpin. Pseudoknots are generally formed in nucleic acid sequences of about 30 to 60 nucleotides. Such intramolecular base pairing is key to the translation of RNA since the presence of pseudoknots can lead to frameshifting either in the 5′ or the 3′ direction (generally designated as −1 or +1) or for allowing read-through. Translational frameshifting allows the expression of alternative translational products in a predictable stoichiometry (ala retroviral or HIV gag-pol fusion peptide); to allow the expression of alternative enzymatic activities; or as a mechanisms for autogenous control (see Farabaugh, 1996, Microbiol Rev. 104).

3. Chemokines

Chemokines are a superfamily of soluble proteins that are involved in immune regulation and in inflammatory processes (such as leukocyte recruitment). Generally, chemokines range in size from about 70 to about 100 amino acids, and in molecular size from about 8 kilodaltons (kD) to about 11 kD. Chemokine like proteins have also been described that are membrane bound (Pan et a., 1997, Nature, 387:611). The chemokines share related primary structure, particularly with a conserved motif of four cysteine residues. Early classification of chemokines was based on whether the first two cysteines are adjacent to each other (“CC chemokines”), or are separated by one amino acid (“CXC chemokines”). More recently, chemokines with a single “C” motif (for example lymphotactin) and “CXXXC” motif (for example, neutotactin) have been described. The α-chemokine receptor CXCR4 has been identified as a coreceptor required for HIV entry. The only known natural ligand for CXCR4 has been identified as the CXC chemokine SDF-1. SDF-1 has been shown to inhibit infection of CXCR4 and CD4 expressing cells by T-tropic HIV-1 strains (Oberlin et al., 1996, Nature 382:833-835). Thus, modified versions of chemokines are being tested to determine whether they may be used to block chemokine receptors from binding by HIV.

Kaposi's sarcoma is an AIDS-related malignancy. The Kaposi's sarcoma-associated herpesvirus (KHSV, human herpesvirus 8) has been shown to encode a chemokine receptor (“GPCR”) that is analogous in sequence and chemokine specificity to CXCR2 (Arvantikas et al., 1997, Nature 385:347-349). This is not the only instance in which a virus has apparently pirated a cellular gene encoding either a chemokine or a chemokine receptor. KSHV and Molluscum contagiosum have open reading frames that encode CC chemokines; and Herpesvirus Saimiri, human cytomegalovirus, KSHV, Equine herpesvirus-2, Swine pox virus, and capripox virus have open reading frames encoding chemokine receptors (Murphy, 1997, Nature 385:296-299; Neote et al., 1993, Cell 72:415-425).

4. HIV Proteins

The HIV genome is known to contain 8 open reading frames on the minus strand of the double-stranded DNA intermediate. From the HIV double-stranded intermediate, and from the HIV promoter located in the 5′ LTR, mRNAs of plus strand polarity are transcribed from the minus strand DNA template (see Definitions section herein). Depending on the processing of the transcript, the mRNA may then be translated into one or more viral proteins including Gag, Pol, Vif, Tat, Vpu, Vpr, Rev, Env, and Nef. Additionally, ribosomal frameshifting is employed to enable gag pol protein. Effective transcription from the 5′LTR HIV promoter is dependent on the presence of Tat for transcriptional activation that dramatically increases the levels of viral mRNAs. A possibility was raised that the plus strand of the viral DNA contains a long open reading frame (ORF), located in the region of the genom complementary to the env gene sequence, that may encode a viral protein of 190 amino acids and a molecular mass of 20 kilodaltons (Miller, 1988, Science 239:1420-1422). However, it is not apparent whether this possibility was confirmed, such as by the demonstration of the putative protein or its respective mRNA. In fact, it is noted in the publication that it is possible that the ORF does not represent a true gene sequence. The possibility that bidirectional transcription occurs in HIV was further evaluated by Michael et al. (1994, J. Virol. 979-87).

Accordingly, there has been and continues to be a long-felt need for the identification of novel HIV proteins which play a role in AIDS pathogenesis, and thus may be important targets of therapeutic intervention.

SUMMARY OF THE INVENTION

The present invention relates to the discovery of a novel gene comprising a open reading frame (ORF) in the plus strand of the viral DNA, and located in the HIV LTR. An antisense initiator element initiates production by RNA polymerase of RNA transcripts of negative strand polarity (antisense RNA) utilizing the plus strand DNA as a template. Thus, using this mechanism, the novel HIV gene is transcribed by the cellular transcriptional apparatus. The gene encodes a protein that is related to, and has a structural motif resembling that of a chemokine. More particularly, the protein has similarity to the chemokine family of proteins. These objects and further features and advantages of the invention will be better understood from the description of the preferred embodiments when considered in relation to the figures.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1a is a schematic representation of the HIV genome illustrating the position of the HIV chemokine-like gene in relation to other HIV genes and regulatory sequences (Meyers et al., 1995, A compilation and analysis of nucleic acid and amino acid sequences, Los Alamos National Laboratory, Los Alamos, N.M.).

FIG. 1b is a schematic representation of the LTR region of HIV illustrating the position of antisense RNA initiation.

FIGS. 2a and 2 b are schematic illustrations of the 5′ LTR of HIV and the templates derived therefrom for in vitro transcriptions.

FIG. 3a and 3 b are representations of the results of in vitro transcription reactions using a eukaryotic transcription system and the templates illustrated in FIGS. 2a and 2 b.

FIG. 4 is a representation of the results of in vivo transcription reactions followed by analysis of RNA using reverse transcription and polymerase chain reaction in Jurkat T cells transfected with the HIV LTR CAt vector or control transfections.

FIGS. 5a and 5 b are representations of the isolation of RNA transcripts originating off of the antisense initiator in stably transfected cells.

FIG. 6 is a schematic representation of the HIV-1 LTR showing various regulatory elements and bidirectional transcription initiation sites, as well as primers utilized in RNA analysis by RT-PCR.

FIG. 7 is a schematic representation illustrating sequence analysis and alignment between amino acids of an HIV chemokine and other chemokines.

FIG. 8 is a schematic representation illustrating sequence alignment between amino acids of HIV chemokines from various cell lines and patient HIV isolates.

FIG. 9 is a schematic representation illustrating the sequence and presence of pseudoknots.

FIG. 10A-10F are photomicrographic representations of the effect of transfection of a HeLa cell line with constructs containing the HIV LTR region.

DETAILED DESCRIPTION OF THE INVENTION

Definitions

By the term “operably linked” is meant, for the purposes of the specification and claims to refer to the chemical fusion (enzymatic restriction with subsequent ligation) or synthesis of heterologous DNA with a nucleotide sequence that encodes an HIV chemokine such that the resultant recombinant DNA molecule is formed in a proper orientation and reading frame for the nucleotide sequence to be transcribed into functional RNA. In the construction of the recombinant DNA molecule, it is generally preferred to position a promoter at a distance upstream from the initial codon of the nucleotide sequence that is approximately the same as the distance in its natural setting (e.g., as in the HIV genome). However, as known in the art, some variation in the distance can be accommodated without loss of promoter function. Likewise, it is generally preferred to position an enhancer element at a distance upstream from the promoter, or incorporated into the promoter sequences as a promoter element, or located between the promoter and the DNA molecule to be expressed. However, as known in the art, some variation in the placement can be accommodated without loss of the enhancer element's function.

By the term “expression vector” is meant, for the purposes of the specification and claims to refer to a DNA molecule which is operably linked to a nucleotide sequence that encodes an HIV chemokine such that the production of the HIV chemokine is effected in a suitable host. The vector may include, but is not limited to, a plasmid, phage, viral vectors, viral-like vectors, or a potential genomic insert.

By the terms “variant of the nucleotide sequence” or “variant of the gene” or “variant sequence” are meant, for the purposes of the specification and claims to refer to a nucleotide sequence that shares substantial identity (an identity of greater than about 70%, not taking third base degeneracy into account) with the gene encoding HIV chemokine. Such a sequence comparison can be performed using existing software known to those skilled in the art. Variants can be natural variants or variants produced by synthetic or mutagenic means for modifying the disclosed nucleotide sequences. With respect to such variations, and as appreciated by those skilled in the art, because of third base degeneracy, almost every amino acid can be represented by more than one triplet codon in a coding nucleotide sequence. Thus, a variant sequence can be modified slightly in sequence (e.g., substitution of a nucleotide in a triplet codon), and yet still encode its respective gene product of the same amino acid sequence as encoded by the disclosed nucleotide sequences. Further, variant sequences may have minor base pair changes which may result in variation (conservative substitution) in the amino acid sequence encoded. Such conservative substitutions are not expected to substantially alter the biologic activity of the gene product. A conservative substitution or modification of one or more amino acids are such that the tertiary configuration of the protein is substantially unchanged. “Conservative substitutions” is defined by aforementioned function, and includes substitutions of amino acids having substantially the same charge, size, hydrophilicity, and/or aromaticity as the amino acid replaced. Such substitutions, known to those of ordinary skill in the art, include glycine-alanine-valine; isoleucine-leucine; tryptophan-tyrosine; aspartic acid-glutamic acid; arginine-lysine; asparagine-glutamine; and serine-threonine. A variant sequence may contain a modification, being defined functionally as resulting in a deletion or addition or substitution of one or more amino acids which does not impart a substantial change in the HIV chemokine that it encodes; i.e., if the encoded HIV chemokine substantially retains the activity of being a cofactor in binding to a chemokine receptor. Such an encoded HIV chemokine may be referred to as a modified variant of HIV chemokine. Methods for synthetically producing such variant sequences are known to those skilled in the art (see, e.g. U.S. Pat. Nos. 5,403,737 and 5,275,945).

By the terms “consisting essentially of” or “consisting” a nucleotide sequence are meant, for the purposes of the specification and claims to refer to the base pair changes (substitution) in the nucleotide sequence such as a change in the third base of a triplet codon (third base degeneracy) or a change resulting in the encoding of a conservative substitution in the amino acid sequence encoded.

Proteins and peptides are chemical compositions made up of a sequence of amino acid units. By the term “consisting essentially” or “comprising” is meant as a term, with an accepted meaning in the chemical patent practice and for the purposes of the specification and claims, to refer to the inclusion of unspecified amino acids (deletion/addition/substitution) which do not materially affect the basic and novel characteristics of the composition; i.e. conservative substitution or modification of one or more amino acids in that sequence such that the protein or peptide substantially retains the biological activity of being a cofactor in binding to a chemokine receptor (“substantially retains” is defined as 50% or more of such biological activity as exhibited by HIV chemokine from an HIV clinical isolate).

By the term “similarity” are meant, for the purposes of the specification and claims to refer to amino acids that are not identical, but similar (amino acids having substantially the same charge, size, hydrophilicity, and/or aromaticity) between two amino acid sequences as determined by sequence comparisons performed using algorithms known to those skilled in the art.

By the term “identity” are meant, for the purposes of the specification and claims to refer to amino acid positions that are identical between two amino acid sequences as determined by sequence comparisons performed using algorithms known to those skilled in the art.

By the term “individual” is meant, for the purposes of the specification and claims to refer to any mammal, especially humans.

By the term “regulatory element” is meant, for the purposes of the specification and claims to refer to an promoter element motif which functions to facilitate binding or recruitment of RNA polymerase or transcription factors in the initiation, activity, and efficiency, of transcription. Eukaryotic regulatory elements include, but are not limited to an antisense initiator, an ATF site, TATA box, a TATA-like box (e.g., TTTAA, TTTAAA, TAT, TAATA), a CAAT box, a CAAT-like box (e.g., CTAATC), upstream stimulatory factor (USF), upstream sequence element (USE), and binding sites for transcription factors (e.g., AP-2, SP1, CRE, PEA-3, NF-IL6, NF-Kβ etc.).

By the terms “HIV Chemokine-like Protein” or “HIV-chemokine” is meant, for the purposes of the specification and claims, to refer to a protein having the following distinguishing and functional characteristics:

(a) a protein encoded by an HIV antisense open reading frame which encodes domains having at least 10% homology to amino acid sequences of chemokines.

(b) is expressed by strains of HIV in at least one phase of virus replication, and is encoded by an open reading frame in the plus strand of the viral dsDNA intermediate, and located in the LTR region.

The term, “Chemokines” includes, but is not limited to, CC chemokines, CXC chemokines, single C motif chemokines (e.g. lymphotactin), CXXXC chemokines (e.g. neurotactin). The chemokine may be membrane bound or secreted.

By the terms “isolated and purified” and “substantially free from other proteins” is meant, for the purposes of the specification and claims, to refer to an HIV chemokine protein preparation that appears to be at least approximately 80% pure, and may be up to approximately 99% pure, as, for example, determined by gel electrophoresis, or liquid chromatography.

By the term “target cell” is meant, for the purposes of the specification and claims, to refer to a human cell which is infectable by HIV including, but not limited to, CD4+ cells bearing chemokine receptors, and CD4-negative cells bearing chemokine receptors; and also refers to human or other mammalian cells bearing chemokine receptors which receptors can bind to soluble HIV chemokine.

The present invention is directed to a gene, represented by an open reading frame in the plus strand of the viral ds DNA intermediate of HIV, which encodes a protein designated “HIV chemokine”. One reason that this gene and its gene products remained unknown until the present invention was the lack of discovery and characterization of the antisense initiator element which allows initiation by RNA polymerases of RNA transcripts of negative strand polarity utilizing the plus strand of the HIV dsDNA LTR pro-viral intermediate as a template (U.S. patent application Ser. No. 08/698,652).

It is now established that chemokine receptors act as coreceptors, with CD4, necessary for HIV to enter a target cell. Additionally, certain chemokine receptors (e.g., CXCR4) may act as the primary viral receptor, in the absence of CD4, necessary for HIV to enter a CD4-negative target cell (Endres et al., 1996, Cell 87:745-756). Thus, HIV cofactors that act on their own or in conjunction with gp120 in the binding to the target cell's chemokine receptor represent components critical in HIV pathogenesis. Chemokines, including RANTES, MIP-1α, and MIP-1β, have been shown to bind to the CCR5 chemokine receptor and inhibit infection by HIV. SDF-1 has been shown to bind CXCR4 and inhibit infection by T-tropic HIV-1 strains. Other chemokines, that bind to one or more chemokine receptors that act as either coreceptors or primary viral receptors, are being sought as drug candidates in their natural state. Additionally, such chemokines are being modified to produce versions which may bind to the chemokine receptor, but not act as an agonist (Science 275:1261-1264, 1997; Simmons et. al., 1997 Science 276:276-279).

The unexpected finding that HIV encodes its own chemokine-like protein, and that the chemokine-like protein may act as a cofactor with gp120 in the binding to and entry of HIV to a target cell, is an important consideration for therapeutic intervention. Thus, the peptides derived from the HIV chemokine gene or variants or modified versions of the HIV chemokine may be used to block entry of target cells during various phases of HIV infection and AIDS. Additionally, chemokine receptors may provide a method by which the HIV chemokine may be isolated and purified from HIV. Alternatively, one or more monoclonal or polyclonal antibodies having binding affinity and specificity for the HIV chemokine may be used as affinity molecules immobilized to an affinity matrix for isolation and purification of the HIV chemokine.

Further, the unexpected finding that HIV encodes its own chemokine-like protein provides evidence that the HIV chemokine is involved in at least one of the mechanisms of AIDS pathogenesis. In that regard, there may be biological properties of the HIV chemokine in addition to that of acting as a cofactor with gp120 or an independent ligand for binding to a target cell, in the binding of HIV to and entry of HIV into a target cell. For example, chemokines in general, and more specifically β-chemokines such as MIP-1α and MIP-1β, can be potent chemoattractants for both monocytes and specific subpopulations of lymphocytes (Schmidtmayerova et al., 1996, Proc. Natl. Acad. Sci. USA 93:700-704). Thus, both human β-chemokine expression induced in HIV infection, and the HIV chemokine-like protein, may function to recruit uninfected T cells and monocytes to sites of active viral replication or inflammation.

Such recruitment of uninfected T cells which are CD4+ to sites of active viral replication, such as in the lymph node, may play a role in the decline of CD4+ T cells observed in the progression of AIDS. Such recruitment of mononuclear phagocytes to sites of active viral replication, such as in the brain, with subsequent activation of the mononuclear phagocytes to produce cytokines and NO (nitric oxide), may play a role in tissue pathology such as the neuropathogenesis observed in AIDS (Shapshak et al., 1995, Adv. Exp. Med. Biol. 373:225-238; Bukrinsky et al., 1995, J. Exp. Med. 181:735-745; Achim and Wiley, 1996, Curr. Opin. Neurol. 9:221-225). Additionally, through genetic variation, HIV may be able to control HIV chemokine expression depending on the tissue type in which it is adapting. In that regard, it is noted that GTV present in spinal cord and dorsal root ganglion harbour an LTR population genetically distinct in sequence from that present in other organs including lymph node, spleen, lung, and peripheral blood (Ait-Khaled et al., 1995, AIDS 9:675-683). Such variation in the LTR sequence can include variations in the sequence of the HIV antisense initiator element, and thus the expression of the HIV chemokine from the antisense initiator element. The heterogeneity of the HIV LTR isolated in various tissues may reflect the predominant collection of mutations in the cells infected in those tissues. Thus, an important consideration in treating or preventing AIDS pathogenesis in certain tissues may be to inhibit the HIV chemokine from recruiting lymphocytes and mononuclear phagocytes to sites of active viral replication. Alternatively, the heterogeneity of the HIV LTR may be part of the mechanism whereby the HIV chemokine acquires the capacity to ligand with a chemokine receptor expressed in a specific tissue as illustrated in FIG. 8 (± ribosomal frameshifting). It should be noted that a CNS derived HIV chemokine contains “CC” motif, whereas a LN/spleen contains “XC” chemokine.

Kaposi's sarcoma is a malignancy that is rare in individuals uninfected with HIV, but frequent in (up to 20 percent of) homosexuals with AIDS. Kaposi's sarcoma-associated herpesvirus (KSHV) is thought to be the virus that is the etiologic cofactor of Kaposi's sarcoma in AIDS patients (Kedes et al., 1996, Nat. Med. 2:918-924; Arvanitakis et al., 1997, Nature 385:347-349). Recently, discovered was a chemokine receptor produced by KSHV (“KSHV GPCR”) which may act as a cofactor in AIDS-related malignancies including Kaposi's sarcoma and primary effusion lymphoma (PEL) (Arvanitakis et al., 1997, supra). However, the expression of this chemokine receptor on an KSHV-infected cell is not sufficient to lead to altered growth or neoplastic transformation. Rather, signaling of cell-KSHV GPCR is required by a cofactor produced during AIDS pathogenesis before altered growth or neoplastic transformation is initiated. Epidemiologic data supports this scenario, since KSHV appears to be sexually transmitted but malignancy primarily occurs only in AIDS patients; i.e., a sexually transmitted agent leading to AIDS-related malignancy rather than just a sexually transmitted agent leading to malignancy. While chemokines of the CXC class or CC class have been shown to bind to KSHV GPCR (Arvanitakis et al., 1997, supra), a logical cofactor that is HIV-related and thus explains the association between AIDS and malignancies including Kaposi's sarcoma and PEL is the HIV chemokine. That is, the HIV chemokine and KSHV GPCR are cofactors that interact to initiate cell signals leading to altered growth or neoplastic transformation in KSHV-infected cells. To interact with the KSHV GPCR which is membrane bound in the KSHV-infected cells, the HIV chemokine may either be soluble (e.g., secreted from HIV-infected cells), or a component of a viral particle or HIV infected cell membrane (e.g., interacting by itself as a membrane bound receptor or in conjunction with gp120).

Alternatively, the HIV chemokine and variants expressed in various tissues or cell lines may represent an ideal vaccine candidate for AIDS prevention in as much as the isolated and purified HIV chemokine (and variants) could be administered as vaccines to stimulate the human individual's intrinsic immune response to a “foreign” HIV chemokine without presumably interfering with human intrinsic chemokines necessary for recruitment of inflammatory responses.

Because the HIV chemokine appears to play an important role for AIDS pathogenesis in vivo, one therapeutic approach is to consider using the HIV chemokine as an immunogen in a vaccine (including multivalent) formulation against disease caused by HIV infection. Thus, isolated and purified HIV chemokine, or peptides made by enzymatically cleaving HIV chemokine or synthesis using the amino acid sequence of HIV chemokine as a reference, may be used as immunogens in various vaccine formulations to prevent HIV entry into target cells, and/or in the prevention of tissue pathology in certain tissues caused by the HIV chemokine's recruitment of lymphocytes and mononuclear phagocytes to sites of active viral replication, and/or to prevent HIV chemokine from interacting with potential chemokine receptors such as KSHV-GPCR.

More specifically, the resultant anti-HIV chemokine-antibodies may function to clear the tissue of chemoattractant HIV chemokine, and/or as “neutralizing” antibodies to block HIV chemokine from acting as a cofactor in binding to chemokine receptors such as for the entry of HIV into target cells or such as expressed by a KSHV-infected cell. Additionally, according to the present invention, the HIV chemokine, or peptides derived therefrom, may be used to generate HIV chemokine-specific antisera (human polyclonal antibody, or human-compatible monoclonal antibody including chimeric antibody) useful for passive immunization in HIV-infected individuals to clear the tissue of chemoattractant HIV chemokine, and/or as “neutralizing” antibodies to block HIV chemokine from acting as a cofactor in binding to chemokine receptors such as for the entry of HIV into target cells or such as expressed by a KSHV-infected cell.

Alternatively, peptides, modified peptides (collectively referred to as “peptides”) or modified variants of HIV chemokine derived from the amino acid sequence of the HIV chemokine may be used as a therapeutic agent. For example, such a peptide (e.g., 7 to 20 amino acids) or modified variant of HIV chemokine may be synthesized so as to minimize inducing an immune response, or have reduced or lack function as a chemoattractant, but retain the receptor binding function of either an antagonist or an agonist. As an antagonist, the peptide or modified variant of HIV chemokine would bind to at least one type of chemokine receptor which acts as a coreceptor or primary viral receptor for HIV entry or associated with AIDS pathogenesis, thereby blocking subsequent interaction of HIV with a target cell uninfected by HIV. In a preferred embodiment, the antagonist would be able to it bind to and block more than one type of such chemokine receptor (e.g., more than one of CCR5, CXCR4, CCR3, CCR-2b, KSHV GPCR, or any combination thereof). As an agonist, the peptide or modified variant of HIV chemokine would bind to at least one type of chemokine receptor which acts as a coreceptor or primary viral receptor for HIV entry or associated with AIDS pathogenesis, thereby blocking subsequent interaction of HIV with a target cell uninfected by HIV. Additionally, the binding of the agonist to the target cell chemokine receptor would trigger the receptor to signal the cell to downregulate the expression of the chemokine receptor, the same signal generated by binding of a chemokine to its receptor (see, e.g., chemokine agonist in receptor binding—Hunter et al., 1995, Blood 86:4400-4408). In a preferred embodiment, the agonist would be able to bind to and block more than one type of such chemokine receptor (e.g., more than one of CCR5, CXCR4, CCR3 or CCR-2b, or any combination thereof). In using such a peptide or modified variant of HIV chemokine, it is noted that human testing of a MIP-1α variant (BB-10010) in cancer and HIV studies seems to be well tolerated and not inflammatory (Lord et al., 1996, Br. J. Cancer 74:1017-1022).

As reviewed above, HIV chemokine production may be modulated, depending upon the tissue type to which it has adapted. Thus, isolated and purified HIV chemokine, or peptides derived therefrom, may be used as an antigen in diagnostic immunoassays directed to detection of HIV infection for staging or to monitor response to anti-viral therapy by measuring the body fluid (e.g., serum, cerebral spinal fluid (CSF), or urine) titer of any anti-HIV chemokine antibody that may be present in the HIV-infected individual. Also, isolated and purified HIV chemokine, or peptides derived therefrom, may be used to generate HIV chemokine-specific antibody which may be useful as reagents for diagnostic assays directed to detecting the presence of HIV chemokine in clinical specimens. Measurements of chemokine levels for chemokines that are cell differentiation-associated (Vinante et al., 1996, Haematologica 81:195-200), or for monitoring efficacy of therapy (Segawa et al., 1996, Intern. Med. 35:155-158) have been described previously. Alternatively, reverse transcription-nucleic acid amplification reactions with primers specific for amplifying all or a portion of the HIV chemokine sequence may be utilized to detect the presence of the HIV chemokine sequences in clinical specimens for staging or to monitor response to anti-viral therapy. Similar methods of nucleic acid amplification have been described previously for determining cell type-specific heterogeneity of the HIV-1 V3 loop in HIV-infected individuals (Yamashita et al., 1994, Virology 204:170-179); or to monitor the LTR variation (Ait-Khaled et al., 1995, supra).

For purposes of the description, the methods and compounds of the present invention will be illustrated in the following examples.

EXAMPLE 1

A gene encoding an HIV chemokine according to the present invention can be obtained by isolating the HIV dsDNA intermediate from an HIV-infected cell, or may be synthesized in vitro by reverse transcriptase-nucleic acid amplification from the antisense MRNA originating from the HIV antisense initiator, HIVaINR. FIG. 1 illustrates the position of the HIV chemokine gene in relation to other HIV genes and regulatory elements.

Alternatively, since the HIV chemokine gene is coded for by the plus strand of the HIV, which is complimentary to the minus strand, the sequence of a given strain of HIV chemokine gene can be deduced from the known LTR region sequences of HIV strains available in gene databanks (see also Human retroviruses and AIDS 1995, a compilation and analysis of nucleic acid and amino acid sequences. Ed. G. Mayers., Los Alamos National Laboratory). To further illustrate this embodiment, the nucleotide sequence of the antisense gene encoding the HIV chemokine of lb4l revINRold was deduced (SEQ ID NO:1) utilizing the nucleotide sequence of the HIV minus strand. This sequence termed as “HIV chemokine gene” has an antisense initiator, aINR, at position 60-68 (SEQ ID NO:1). Tha aINR has the consensus as disclosed in our application Ser. No. 08/853,703, now U.S. Pat. No. 5,919,677. A TATA box is present about 42 nucleotides downstream from the site of antisense initiation and in the opposite orientation at nucleotides 110-114. There is also an ATF consensus site upstream of the antisense gene. The open reading frame encodes a protein of 81 amino acids (SEQ ID NO:2). The production of this protein requires a frameshift at the nucleotide at position 263 of SEQ ID NO:1. The frameshifting is potentiated by the formulation of pseudoknot structures in the RNA. The lbl revlNkold sequence is derived from pNLgag (Adachi et al., J. Virology, 59:284-291) which has a mutation following the first start codon of HIV chemokine at nucleotide 114 such that a stop codon immediately follows. Therefore, the second start site at nucleotide 206 is utilized. However, most other HIV strains actually have the first start codon available and potentially viable, which would entail sets of ribosomal frameshifts and code for larger proteins.

In another illustration of this embodiment the nucleotide sequence of the antisense RNA encoding HIV chemokine of SF-2 strain of HIV was deduced (SEQ ID NO:6) from the known nucleotide sequence of the minus strand. The first start codon is at nucleotide 52. The second start codon is at nucleotide 144. The larger protein (SEQ ID NO:7), starting at the first start codon has 112 amino acids and requires a (+1) frameshift at nucleotide 133 and −1 ribosomal frameshift at nucleotide 265. Another large protein (SEQ ID NO:14) is obtained by a (−1) frameshifting at nucleotide 133 and a (+1) frameshifting at nucleotide 265. If the sequence is read through, a protein of SEQ ID NO:15 is possible. Two shorter proteins are also possible starting at the second start codon. The first of these two (SEQ ID NO:8) has 82 amino acids and requires two (−1) ribosomal frameshifts at nucleotide 200 and nucleotide 265. The second of the shorter proteins (SEQ ID NO:9) has 81 amino acids and requires a ribosomal frameshift at nucleotide 201. It should be noted that both a 5′ terminal hairpin, as well as pseudoknot motifs are present within the HIVaINR-generated antisense RNA (FIG. 9). These pseudoknots closely resemble synthetic RNA pseudoknots selected for binding to HIV-reverse transcriptase (Tuerk et al., 1992, Proc. Natl. Acad. Sci. USA, 89;6988-6992). Similarly, sequences of antisense RNA of other strains of HIV can be deduced from the nucleotide sequence of the minus strand. These sequences are found to display at least 80% homology to the sequence of SEQ ID NO:6.

To further illustrate this embodiment, the nucleotide sequence of the antisense RNA encoding HIV chemokine of a HIV strain isolated from the CNS of a patient was deduced from the known nucleotide sequence of the minus strand (SEQ ID NO:25). The first start codon is at nucleotide 52. Depending upon the frameshifting or readthrough, multiple proteins are possible. For a (+1) frameshift at 133 nucleotide and (−1) frameshift at nucleotide at 265, a protein of SEQ ID NO:10 is obtained. For a ribosomal frameshift of (−1) at nucleotide at 133, and a (+1) frameshift at nucleotide, a protein of SEQ ID NO:11 is obtained.

In another illustration, the nucleotide sequence of the antisense RNA encoding HIV chemokine of a HIV strain isolated from the lymph node and spleen of a patient was deduced from the known nucleotide sequence of the minus strand (SEQ ID NO:26). The first start codon is at nucleotide 52. Depending upon the frameshifting or readthrough, multiple proteins are possible. For a (+1) frameshift at 133 nucleotide and (−1) frameshift at nucleotide at 280, a protein of SEQ ID NO:12 is obtained. Additional amino acids are coded for in some variants. For a ribosomal frameshift of (−1) at nucleotide at 133, and a (+1) frameshift at nucleotide 280, a protein of SEQ ID NO:13 is obtained.

Similarly, amino acid gequences for chemokine-like proteins from other strains of HIV can be obtained from the antisense RNA sequence. Thus, the amino acid sequence for (+1), (−1) frameshift for YU2 strain is disclosed in SEQ ID NO:16 and the amino acid sequence for (−1), (+1) frameshift is dislosed in SEQ ID NO:17, while the amino acid sequence obtained by readthrough is SEQ ID NO:18.

The amino acid sequence of a chemokine-like protein for ELI strain with read through is disclosed in SEQ ID NO:19.

The amino acid sequence of a chemokine from another strain, p896, with several readthrough events is disclosed in SEQ ID NO:20.

It should also be noted that constructs which contain HIV LTR regions may also be used to produce HIV chemokines-like proteins. For example, the antisense RNA sequence of pHIV-CAT which is commonly used to transfect cells and was used to transfect cells as disclosed herein was obtained by standard sequencing techniques and is disclosed in SEQ ID NO:21. This antisense RNA encodes proteins of SEQ ID NO:22, SEQ ID NO:23, and SEQ ID NO:24.

From these illustrations it will be evident to those skilled in the art that the sequence of the antisense RNA encoding chemokine-like proteins from HIV strains or double stranded constructs derived from the HIV strains, can be deduced. It will also be appreciated by those skilled in the art that the plasticity of the HIV genome leads to variations in the antisense RNA sequence. Such variations are intended to be included within the scope of this disclosure. Ribosomal frameshifting adds another element of plasticity to the sequence of encoded protein and is also intended to be within the scope of this disclosure.

In another illustration of this embodiment, the HIV chemokine gene including the open reading frame and HIV chemokine encoding sequence from different strains of HIV can be isolated. HIV dsDNA intermediate from an HIV-infected cell can be isolated or RNA transcripts may be amplified in vitro by reverse transcription from the HIV RNA by using oligonucleotide primers which specifically hybridize to the nucleotide sequence of SEQ ID NO:1. Using this sequence, it will be appreciated that one skilled in the art may design oligonucleotide primers useful in the nucleic amplification of the HIV chemokine gene, or oligonucleotide probes useful for detection of amplified sequences containing all or a portion of the HIV chemokine-like protein encoding sequence in other strains of HIV isolated from different individuals or of HIV isolated from different tissues of the same individual.

A further alternative is to isolate either HIV RNA or HIV dsDNA from HIV-infected cells using methods known to those skilled in the art, and then use techniques that would result in the amplification and/or cloning of an HIV chemokine coding sequence. Following determination of the nucleotide sequence of the isolated HIV chemokine, further characterization may be performed by computer analysis using software known in the art to record the DNA sequence and determine the correct reading frame, codon usage, predicted amino acid sequence and molecular size of the encoded HIV chemokine, and comparison of the amino acid sequence of that particular HIV chemokine with the amino acid sequence of other HIV chemokines (FIG. 7).

EXAMPLE 2

This embodiment illustrates the generation of HIV chemokine RNA transcripts off of the antisense initiator, HIVaINR. Since HIV-1, once integrated into a human host cell chromosomal DNA, is dependent upon eukaryotic transcription factors and RNA polymerases to transcribe its genes (Cullen, 1992, Microbiol. Reviews, 375-394), a eukaryotic transcription system (commercial Drosophila embryo nuclear extract transcription system) that can efficiently transcribe from eukaryotic initiators in vitro was used to investigate whether eukaryotic transcription could initiate from the HIVaINR. Four different HIV-1 LTR fragments, illustrated in FIG. 2a, were generated by polymerase chain reaction using HIV-LTR templates and primers containing bacteriophage T7 or Sp6 polymerases, as previously described (Ludwig et al., 1995, Nuc. Acid Res. 23:3792-3793), which method is hereby incorporated by reference. The fragments are 5′Hae III PBS (Sp6) 3′ which includes two Sp1 sites and TATA box and extends through the primer binding site (PBS; Fragment 1); 5′ PvuII-PBS (Sp6) 3′ fragment which lacks all of the Sp1 sites and bisects the TATA box (Fragment 2); 5′ (T7) PvuII-SacI (Sp6) 3′ fragment which truncates the TAR region 48 base pairs from the mRNA cap site and start site (Fragment 3); and 5′ (T7) R-BssHII (Sp6) 3′ fragment which contains no HIV-1 promoter Sp1 sites or TATA box but contains the TAR region DNA (Fragment 4).

In vitro transcription reactions were performed with each template using a eukaryotic transcription system (Drosophila Nuclear Extract, Promega) according to manufacturer's instructions, to initiate transcription off of HIVaINR. This eukaryotic transcription system used Drosophila nuclear extracts to supply transcription factors and the eukaryotic RNA polymerases. Each of the in vitro transcription reactions was then treated with DNase I to remove DNA template, followed by phenol chloroform extraction and by ethanol precipitation to remove the DNase from the synthesized RNA. The RNA transcripts were hybridized either to a biotin-labeled sense RNA probe (5′ (T7) R-U5-PBS-BssH II (SP6) 3′) FIG. 3a, lane 1-6 or to biotinylated antisense RNA probe (5′ (SP6) BssH II-PBS-U5-R (T7) 3′) FIG. 3a, lanes 10-15. The hybridized RNA was subjected to ribonuclease T1 digestion and analysis by electrophoresis on a denaturing 8% polyacrylamide gel electrophoresis (PAGE). The size of RNA transcript was observed to be 25 nucleotides distinct from the protected TAR loop or undigested probe (FIG. 3a, lanes 2-6; which was absent in control lane 1).

As shown in lanes 10-15, FIG. 3a, no expected size transcripts were initiated in the usual sense orientation, as demonstrated by the failure of the antisense probe to hybridize, and thereby protect, sense transcripts in a RNA digestion assay. It is important to note that for the in vitro transcription experiments, Drosophila nuclear extracts were used, which intrinsically lack Sp1 protein. Thus a major driving force for sense transcription from the HIV-1 promoter in vitro was lacking, enabling the observance of antisense transcription in isolation. It was observed that primer extension utilizing HIV-specific biotinylated primers and unlabeled dNTPs allowed specific analysis of the RNAs synthesized off the HIV LTR templates while eliminating the background contribution seen from the Drosophila nuclear extract (FIG. 3b). Simultaneous in vitro transcription reactions performed using Drosophila nuclear extract and either the original HIV-1 LTR (labeled O), or truncated portions of the HIV-1 LTR extending from the AvaI to the HindIII site. (labeled A), or extending from the AvaII to the HindIII site (labeled B), as diagrammed in FIG. 2b) allowed delineation of the 3′ end of the antisense transcript between the AvaII site and the U3 end of the HIV-1 LTR (FIG. 3b). Control transcription reactions receiving no template were labeled NT. Primer extension with sense AvaI or Ava II primers, with RNA synthesized from the truncated A or B templates demonstrated cDNA of the expected size for an antisense transcript generated off the HIV aINR.

EXAMPLE 3

This embodiment is directed towards demonstration of in vivo transcription from HIV-aINR. An in vivo eukaryotic transcription system may be used to produce mRNA transcripts from human cell lines (e.g., a lymphoid cell line such as Jurkat T cells, or a mononuclear phagocyte cell line) which have been transfacted with a eukaryotic vector containing the coding sequence for HIV chemokine operably linked to the HIV antisense initiator or other functional eukaryotic promoter including one or more regulatory elements.

To further illustrate this embodiment, in vivo transcription from the HIV-aINR was analyzed by reverse transcription-polymerase chain reaction of RNA isolated from human Jurkat T cells which has been transfected with pHIV-CAT. Plasmid pHIV-CAT contains the HIV-1 LTR U3 and R sequences 5′ to the chloramphenicol acetyltransferase (CAT) gene. Transfections of plasmid DNA were performed in the presence of a transfection agent (Transfectam™, Promega). Briefly, plasmid DNA (0.086 μg plasmid DNA per 0.182 μl transfectum per well for 2 hours) was incubated with the cells using conditions as essentially described by the manufacturer. Control transfection reactions included pHIV-CAT plus pSV-βgal plus transfection reagent (to assess transfection efficiency), transfection reagent alone (“mock” transfection), or no treatment at all. Cells were then resuspended in culture medium and continued in culture for two days. RNA was then extracted from the pelleted cells, and purified using standard techniques well known in the art. The purified RNA was then split and subjected to reverse transcription using a 5′ AvaI sense primer (SEQ ID NO:3), to anneal with and extend HIV-antisense transcripts; followed by amplification by PCR with 30 cycles of denaturing (94°, 45 seconds), reannealing (70° C., 45 seconds), and extension (72° C., 2 minutes) using the Ava1 sense primer and either a 3′ antisense primer (SEQ ID NO:4), or a 3′ Mael antisense primer (SEQ ID NO:5). The reverse-transcription-PCR products were then analyzed by 3% agarose gel electrophoresis, transferred to a nitrocellulose membrane (Biodyne) and detected colorimetrically.

The results are illustrated in FIG. 4. The lanes marked “M” represent DNA size standard markers. HIV-1 RNA transcripts could be detected only in RNA isolated from Jurkat T cells transfected with pHIV-CAT (FIGS. 4, 7 a-12 a), using a 5′ sense primer (5′ AvaI) to extend off the antisense transcript in the reverse transcription reaction, followed by PCR amplification with the 5′AvaI sense primer and a biotinylated antisense 3′ 441 primer containing sequences complementary to beginning TAR sequences. As shown in FIG. 4, lanes 1a-3a), no product was obtained in simultaneous identical reverse-transcription PCR reactions performed using total cellular RNA isolated from Jurkat T cells that were mock transfected, and received transfectam but no DNA template (NT). No products were obtained when the same samples as in lanes 7a-12a in FIG. 4, were simultaneously analyzed by reverse transcription PCR with 5′ AvaI in the reverse transcription step, but amplified with an alternative 3′ MaeI antisense primer during PCR (lanes 7b-12b). The 3′ MaeI antisense primer is complementary to sequences in TAR region situated beyond the HIV aINR (FIG. 6), and in therefore, not expected to generate amplified products from authentic antisense RNA. This control, therefore, serves to confirm the authenticity of transcripts originating from the HIVaINR.

In another illustration of this embodiment cells stably transfected with HIV were used to demonstrate the presence of transcripts originating from the HIVaINR. Therefore, cell line U38 containing stably transfected HIV-1 LTR-CAT gene sequences were analyzed for in vivo antisense HIV-1 transcripts. The cells were cultured with or without stimulation with calcium ionophore and phorbol ester. Total RNA was extracted by standard methods, split equally three ways and treated either with a single DNase treatment, two DNase treatments, or two DNase treatments plus RNase digestion. The samples were then subjected to reverse transcription-PCR. For reverse transcription PCR analysis, each treated sample was analyzed five ways: for the presence of antisense HIV-1 transcripts (FIGS. 5a and 5 b, lanes 2-7); for the presence of sense HIV-1 transcripts (FIG. 5a and 5 b, lanes 28-33); for the presence of DNA contamination (FIG. 5a and 5 b, lanes 20-25); for G3PDH RNA (FIG. 5b, lanes 37-42); and for reverse transcription PCR performed without the reverse transcriptase (FIG. 5a and 5 b, lanes 11-16. Internal controls, consisting of primer without template (FIG. 5, “Pr”, lanes 8,17,26,34 and 43) were also run to confirm that the reverse transcription-PCR reaction mixture were not contaminated with templates. A separate control set with primers and an internal control standard RNA template (FIG. 5, “Is”, lanes 1,10,19,27, and 36) was run to confirm comparable primer annealing efficiency. In addition, RT± and PCR (kit) ± kit controls were run in lanes 44-47. Thus, FIG. 5a illustrates the biotin-labeled RT-PCR products following transfer to a membrane and calorimetric detection (G3PDH primers were not labeled), and 5 b illustrates the RT-PCT products as photographed following ethidium bromide staining of the gel prior to transfer.

As shown in FIGS. 5a and 5 b, antisense RNA transcripts are made off of the HIVaINR in stably transfected cells in vivo, at a level (lanes 2-7) comparable to intrinsic cellular G3PDH RNA transcripts (FIG. 5b, lanes 37-42) and sense HIV-1 transcripts (lanes 28-33). RNase digestion (lanes 4 and 7), but not DNase digestion (lanes 2,3,5 and 6) of the U38 total cellular RNA eliminated the antisense RNA product band(s) of reverse transcription-PCR reactions. The identical RNA samples that had RNase treatment also demonstrated the elimination of products for G3PDH RNA (FIG. 5b, lanes 39 and 42, and for sense HIV RNA lanes 30 and 33). Antisense RNA generated off the HIV-1 LTR and analyzed by reverse transcription using sense primer (5′ AvaI) generated a cDNA when the sense 5′ primer or the antisense 3′ 441 primers were present in the PCR reaction but not when an antisense MaeI primer was present in the PCR reaction. The MaeI primer anneals outside of the transcription start site for antisense RNA. Third, while DNA contamination can be observed with U38 total cellular RNA samples obtained from cells stimulated with Ca ionophore and PMA, and treated with DNase only once (FIG. 5a and 5 b, lane 14), no contamination was observed with any of the total cellular RNA samples obtained from unstimulated U38 (FIG. 5a and 5 b, lanes 11-13, which correspond to the same RNA samples analyzed in lanes 2,-4).

In summary, this embodiment demonstrates the generation of authentic antisense transcripts in vitro and in vivo.

EXAMPLE 4

An HIV chemokine according to the present invention may be characterized by its amino acid sequence, which may vary depending on the HIV isolate of origin, including tissue site of the HIV isolate of origin. By using nucleotidesequence data, the amino acid sequence of the HIV chemokine protein, as shown in SEQ ID NO:2 for lbl revINRold, SEQ ID NOs: 7,8 and 9 for SF-2 strain is derived.

In one illustration of this embodiment, using a gene database, and a software alignment program known in the art, a sequence comparison was made between a HIV chemokine amino acid sequence and various mammalian chemokines. FIG. 7 illustrates a comparison of the deduced amino acid sequence of HIV chemokine of the present invention and other chemokines. After introducing gaps in the SDF-1 sequence, a consensus was obtained for 23 of the amino acids of HIV chemokine (lbl revINRold; SEQ ID NO:2) and SDF-1; for 20 of the amino acids of HIV chemokine (lbl revINRold; SEQ ID NO:2) and IL8-human, and HIV chemokine and I-309 (FIG. 7). The α-chemokine receptor CXCR4 has been identified as a coreceptor required for HIV entry, and one natural ligand for CXCR4 has been identified as CXC chemokine SDF-1. Thus, the relatedness of the HIV chemokine to SDF-1, as shown in FIG. 7, implicates the HIV chemokine as being a factor (alone) or a cofactor (with gp120) in binding to chemokine receptors required for HIV entry into a target cell. That SDF-1 has been shown to inhibit infection of CXCR4 and CD4 expressing cells by T-tropic HIV-1 strains (Oberlin et al., 1996, supra) suggests that isolated and purified HIV chemokine may also inhibit infection of CXCR4 and CD4 expressing cells by HIV-1 strains. Based on these findings, the HIV chemokine may be used to generate peptides or a modified variant of the HIV chemokine for use as a vaccine; as an antigen to generate antisera such as for neutralizing antibodies and for diagnostic immunoassays; as an agonist of HIV chemokine; as an antagonist to HIV chemokine and to generate primers or probes from the corresponding HIV chemokine coding sequence for diagnostic and prognostic applications.

In another illustration of this embodiment, the amino acid sequences of HIV chemokines from different strains of HIVs was deduced from their known nucleotide sequences of the minus strand available from gene databases. Using commercially available software, the amino acid sequence of HIV chemokines transcribable from the plus strand was compared for cell lines and HIV isolates from patients. The cell lines compared were TCLA, SF-2, macrophage trophic primary viral (YU2). The data from HIV isolates of patients was obtained from either central nervous system ((Pt)CNS) or lymph node and spleen isolates ((Pt)LN/SP. As illustrated in FIG. 8, the amino acid sequence of the HIV chemokines shows a high degree of homology with the N-terminus being more conserved. Although the amino acids comprising this portion of the amino terminus of all HIV chemokines analyzed to date seem to be conserved, one skilled in the art will appreciate that minor variations in the amino acid sequence may occur, particularly since HIV is known to frequently vary its sequences. However, the comparison suggest that the conservation of this region may reflect a common mechanism for structure (e.g., folding) or for regulation. The plasticity of the RNA (secondary tertiary structures i.e. pseudoknots) enables more than one potential reading frame to be utilized.

EXAMPLE 5

The present invention relates to an HIV gene, isolated from a strain of HIV, wherein the gene encodes an HIV chemokine-like protein. With sequence information, like that shown in SEQ ID NOs: 1 and 2, other polypeptides can be produced which display “HIV chemokine” activity. More particularly, variant nucleotide sequences can be natural variants or variants produced by synthetic or mutagenic means for modifying the disclosed nucleotide sequences. Methods for synthetically producing such variant sequences are known to those skilled in the art of protein design. In designing such variants, one needs to consider avoiding mutations of sequences that encode the structurally and functionally-involved amino acids, or the cysteine residues involved in disulfide bond formation, which may negatively affect the role of the HIV chemokine in binding to chemokine receptors. In that regard, it is noted that the receptor-binding pocket (also called the “hydrophobic pocket”) is a domain of the HIV chemokine involved in binding to chemokine receptors. The domain can be determined using methods known in the art in which chimeras of chemokines, in which domains are interchanged, are tested for their ability to bind to a specific receptor (Heinrich and Bravo, 1995, J. Biol. Chem. 270:28014-7; Hammond et al., 1996, J. Biol. Chem. 271:8228-35). These standard techniques have been used to determine which binding domain(s) can function as an agonist, partial agonist, or an antagonist (Heinrich and Bravo, 1995, supra). Thus, the potential domains of HIV chemokine, resembling that of other chemokines can be interchanged with similar domains of SDF-1 in forming chimeras whose binding specificity to CXCR4 (or CXCR4 and CD4) expressing cells can then be evaluated using methods known in the art (Oberlin et al., 1996, supra, Bleul et al., 1996, supra). Similarly, chimeras made of domains of HIV chemokine with another chemokine (e.g., RANTES or MIP-1α, or MIP-1β) and tested against β-chemokine receptor expressing cells (CCR-5, or CCR2b, or CCR3) may be used to determine the domain(s) of HIV chemokine that can function as an agonist, partial agonist, or an antagonist. Analysis of chimera binding to β-chemokine receptor expressing cells has been described previously (see, e.g., Rucker et al., 1996, Cell 87:437-446). Identifying the amino acids making up a HIV chemokine functional domain in binding specificity to a chemokine receptor enables the design of peptides or modified variant HIV chemokine which may be useful for therapeutic and/or diagnostic applications.

In one embodiment, the variant sequence may be produced by site-directed mutagenesis using one of the several methods for such mutagenesis which are known to those skilled in the art (see, e.g. U.S. Pat. No. 5,397,705). For example, site directed mutagenesis using oligonucleotides comprises the steps of (i) synthesizing an oligonucleotide with a sequence nearly identical to a sequence in the HIV chemokine gene except that the oligonucleotide sequence contains the desired nucleotide substitution (encoding for a mutation in the amino acid sequence); (ii) hybridizing the oligonucleotide primer to a template comprising the nucleotide sequence encoding an HIV chemokine; and extending the oligonucleotide primer using a DNA polymerase. The resultant variant sequence may then be incorporated into an expression vector which is then used to genetically engineer a host cell to recombinantly produce a polypeptide having at least partial, if not full, HIV chemokine binding specificity.

In another embodiment, genetic engineering techniques can be used to generate nucleic acid molecules comprising a variant sequence that is a substantial portion of the HIV chemokine gene. As apparent to one skilled in the art, from the HIV chemokine gene sequence, and from a restriction map thereof, it can be determined which restriction enzyme or combination of restriction enzymes may be used to generate nucleic acid molecules encoding a modified variant of HIV chemokine having some of, the same as, or more than, the binding specificity exhibited by the HIV chemokine of natural HIV isolates. Restriction enzyme selection may be done so as not to destroy the binding domain/hydrophobic pocket of the resultant polypeptide. Consequently, restriction enzyme combinations may be used to generate nucleic acid molecules (variant sequences), which when inserted into the appropriate vector, are capable of directing the production of a modified variant of HIV chemokine having some of, the same as, or more than, the binding specificity exhibited by the HIV chemokine of natural HIV isolates.

In a further embodiment, an HIV chemokine may be made into a modified variant of HIV chemokine by chemical means. For example, a modified variant (a “derivative”) of the chemokine RANTES was created by chemical modification of the amino terminus (Simmons et al., 1997, Science 276:276-279). The amino terminus was modified by reacting it with aminooxypentane (AOP). The resultant AOP-RANTES was a potent antagonist which inhibited infection of target cells by M-tropic HIV-1 strains (indicating full receptor occupancy), yet did not induce chemotaxis. Thus, the amino terminus of HIV chemokine may be reacted with AOP by amino terminal oxidation using the methods described by Simmons et al. (supra) to achieve a modified variant of HIV chemokine that may act as an antagonist.

EXAMPLE 6

This embodiment illustrates that a nucleic acid molecule comprising a nucleotide sequence encoding an HIV chemokine, a variant sequence encoding a modified variant HIV chemokine, or a nucleotide sequence encoding a peptide derived from HIV chemokine (collectively referred to as “nucleotide sequence), can be inserted into a vector for expression in a host cell system. Successful expression of the HIV chemokine, modified variant HIV chemokine, or peptide derived from HIV chemokine (collectively referred to as “recombinant HIV chemokine”), requires that either the insert comprising the nucleotide sequence encoding the recombinant HIV chemokine, or the vector itself, contain the necessary elements for transcription and translation (regulatory elements) which is compatible with, and recognized by the particular host system used for expression. A variety of host systems may be utilized to express the recombinant HIV chemokine, which include, but are not limited to bacteria transformed with a bacteriophage vector, plasmid vector, or cosmid DNA; yeast containing yeast vectors; fungi containing fungal vectors; insect cell lines infected with virus (e.g. baculovirus); and mammalian cell lines transfected with plasmid or viral expression vectors, or infected with recombinant virus (e.g. vaccinia virus, adenovirus, adeno-associated virus, retrovirus, etc.).

Using methods known in the art of molecular biology, including methods described above, the antisense initiator, aINR, or other promoters and regulatory elements can be incorporated into the vector or the nucleotide sequence encoding the recombinant HIV chemokine, to increase the expression of the recombinant HIV chemokine, provided that this increased expression is compatible with (for example, non-toxic to) the particular host cell system used. The selection of the promoter will depend on the expression system used. Promoters vary in strength, i.e. ability to facilitate transcription. Generally, for the purpose of expressing a cloned gene, it is desirable to use a strong promoter in order to obtain a high level of transcription of the nuclectide sequence and expression into the recombinant HIV chemokine product. For example, bacterial, phage, or plasmid promoters known in the art from which a high level of transcription has been observed in a host cell system comprising E. coli include the lac promoter, trp promoter, tac promoter, recA promoter, ribosomal RNA promoter, the P_(R) and P_(L) promoters, lacUV5, ompF, bla, 1pp, and the like, may be used to provide transcription of the inserted nucleotide sequence encoding the recombinant HIV chemokine. Promoters known in the art for transcription to occur in mammalian cells may include viral or viral-like basal promoters like the SV40 late promoter, the RSV promoter, the CMV immediate early promoter, adenovirus major late promoter, the MMTV promoter, and a VL30 promoter; and cellular promoters including metallothione promoters (See, e.g., Larsen et al., 1995, Nucleic Acids Res. 23:1223-1230; Donis et al., 1993, BioTechniques 15:786-787; Donda et al., 1993, Mol. Cell. Endocrinol. 90:R23-26; and Huper et al., 1992, In Vitro Cell Dev. Biol. 28A:730-734), and may be used to provide transcription of the inserted nucleotide sequence encoding the recombinant HIV chemokine.

Other regulatory elements for efficient gene transcription or message translation include enhancers, and regulatory signals. Enhancer sequences are DNA elements that appear to increase transcriptional efficiency in a manner relatively independent of their position and orientation with respect to a nearby gene. Thus, depending on the host cell expression vector system used, an enhancer may be placed either upstream or downstream from the inserted nucleotide sequence encoding the recombinant HIV chemokine to increase transcriptional efficiency. One or more regulatory elements, such as transcription or translation initiation signals, may be used to regulate the expression of the nucleotide sequence encoding the recombinant HIV chemokine. Such regulatory elements may be inserted into the nucleotide sequence encoding the recombinant HIV chemokine or nearby vector DNA sequences using recombinant DNA methods described for insertion of DNA sequences.

Accordingly, a nucleotide sequence encoding for a recombinant HIV chemokine can be ligated into an expression vector at a specific site in relation to the vector's promoter and regulatory elements so that when the recombinant vector is introduced into the host cell, the recombinant HIV chemokine is expressed from the recombinant vector in the host cell. For example, the nucleotide sequence containing its own regulatory elements can be ligated into an expression vector in a relation or orientation to the vector promoter, and control elements which will allow for expression of the recombinant HIV chemokine. The recombinant vector is then introduced into the appropriate host cells, and the host cells are selected, and screened for those cells containing the recombinant vector. Selection and screening may be accomplished by methods known in the art including detecting the expression of a marker gene (e.g., drug resistance marker or auxotrophic marker) present in the vector; immunoscreening for production of recombinant HIV chemokine-specific epitopes using antisera generated to epitopes of HIV chemokine; probing the DNA of the host cells for a nucleotide sequence encoding a recombinant HIV chemokine using one or more oligonucleotides, and methods known in the art; and a functional assay to test binding of the recombinant HIV chemokine to a chemokine receptor which is known to bind to HIV chemokine.

EXAMPLE 7

This embodiment demonstrates the effects of introducing the gene sequence for the HIV chemokine(s) into a cell line. To illustrate this embodiment, a cell line stably producing multiple HIV-1 proteins but no infectious virus was used (HL2/3; Ciminale et al., 1990, AIDS Research and Human Retroviruses, vol 6, p 1281-1286). HL2/3 was generated by stably transfecting HeLa cells with a hybrid HIV-1 clone HXB2/3gpt and selecting for stable production of HIV-1 proteins. Gag, Env, Tat, Rev, and Nef, but no reverse transcriptase, are produced by this cell line and co-cultivation experiments demonstrate no viral propagation. It was intended as a fusion partner, along with another cell line expressing CD4 (HLCD4-CAT). No CD4 is expressed on the surface of the HL2/3 cell line as determined by flow cytometry.

HeLa cells (3.8×105/well) were plated and then transfected the following day for 2 hours, followed by the addition of serum containing media and various treatments. A comparison of cells following either mock transfections (Transfectam, Promega) or transfections with either pHIV-CAT (abbreviated PHIV; Nable et al., 1987, Nature, 326:711-713), or pwtΔ (Rizzuto et al., 1998, Science, 280:1949-53 and pHIV-CAT (abbreviated as pHIV+pwt) performed as described in Example 3, illustrates the effects of the HIV-1 LTR U3 and R sequences (containing the HIV chemokine gene) on cell survival and morphology (Table 1 and FIG. 10). Sequencing of the constructs indicated that plasmid pHIV-CAT contains the HIV-1 LTR U3 and R sequences 5′ to the CAT gene, whereas the plasmid pwtΔ contains a truncated gp-120 construct (Sodroski et al.) as well as the HIV-1 LTR. HL2/3 cells, following transfection, were ± stimulated with Ca ionophore (50 ng/ml) and phorbol myristate acetate (50 ng/ml) or treated or not with affinity-purified rabbit antibody to HIV chemokine peptides (+Ab) and grown on coverslips for hematoxylin and eosin staining in 6-well plates. Four peptides were used together for generating the antibodies. These were peptide corresponding to amino acid 19-35 of SEQ ID NO:10, amino acid 51-71 of SEQ ID NO:2, amino acid 89-103 of SEQ ID NO:10 with a cysteine at N-terminal end, and amino acid 20-38 of SEQ ID NO:2. After 3 days, the coverslips were removed for staining and cell counts and viability were assessed by trypan blue exclusion. Cell morphology was assessed by phase contrast microscopy in the well and following staining (FIG. 10).

TABLE 1 TOTAL CELLS × 10⁵/ALIVE × % GROUP TREATMENT 10⁵ DEAD COMMENTS 1 Mock, 4.6/4.5 1 normal HeLa unstim. 2 Mock, 9.7/9.5 1 normal HeLa; unstim; Ab increased 3 Mock, stim 7.1/6.9 1 normal cellular +Ab +/−clumps 4 pHIV, stim 5.1/2.8 45 pyknotic cells, +Ab giant cells 5 pHIV + pwt, 3.6/1   72 ++clumps, stim +Ab pyknotic, syncytium 6 Mock, stim 2.1/2.0 2 less cellular, few mitosis 7 pHIV, stim 1.3/1.1 15 less cellular, +/−pyknotic 8 pHIV + pwt, 1.2/0.9 25 +clumps, stim pyknotic

When representative coverslips from the above groups were stained and examined the following observations were made. Mock stimulated cells (Group 6; FIG. 10A) were present in a monolayer with relatively uniform round to oval nuclei, low nuclear to cytoplasm ration, abundant stellate amphophilic cytoplasm with cytoplasmic processes. Cellular nuclei contained finely granular, evenly distributed chromatin (1-3 prominent nucleoli). Scattered binucleated cells were also observed. For pHIVCAT transfected and stimulated cells (Group 7; FIG. 10B); viable cells with nuclear and cytoplasmic features similar to those in control (FIG. 10A) were observed. However, there were numerous degenerated cells that contained pyknotic, shrunken nuclei and eosinophilic cytoplasm (apoptotic). For pHIVCAT+pwtΔ transfected and stimulated cells (Group 8; FIG. 10C), only a few cells were present. A single syncytium is shown in FIG. 10C consisting of pyknotic nuclei and eosinophilic cytoplasm. Some nuclei with partially clumped chromatin can also be seen.

For mock transfected, stimulated cells that received antibody to peptides 1-4 (Group 3; FIG. 10D), cells were in a monolayer and similar to Group 6. However, the cytoplasm appeared more vacuolated, and nucleoli were prominent and angulated. FIG. 10D shows a single quadripolar mitotic figure. For cells transfected with with pHIVCAT+pwtΔ, stimulated, and receiving antibody (Group 5; FIG. 10E), syncytium was present but the nuclei were all shrunken and pyknotic. The nuclear to cytoplasmic border was not discernable. Some of the uninucleate cells appeared to have somewhat shrunken nuclei containing condensed chromatin suggestive of degeneration. In an additional set of cells transfected with pHIVCAT+pwtΔ, stimulated and receiving antibody, soluble CD4 was added (FIG. 10F). Prominent syncytium with multiple nuclei containing prominent angulated nucleoli and vacuolated cytoplasm.

These data indicate that the addition of constructs that can generate antisense RNA encoding chemokine-like proteins to a HeLa cell line that expressed the HIV proteins HIV-1 proteins, Gag, Env, Tat, Rev, and Nef, but no reverse transcriptase, resulted in cell degeneration and death. Additional expression of gp120 increased the effect indicating that gp120 may be acting in association with the chemokine-like protein. These results further indicate that a chemokine-like protein is produced from the antisense RNA transcribed off of the antisense initiator in HIV.

EXAMPLE 8

This embodiment illustrates that a recombinant HIV chemokine encoded by a nucleotide sequence according to the present invention can be purified from the host cell expression system using an affinity molecule such as by affinity chromatography. Also this embodiment illustrates using an affinity molecule to purify HIV chemokine from cells infected with HIV. An affinity molecule is a molecule that has binding specificity to the recombinant HIV chemokine or HIV chemokine from infected cells. Such an affinity molecule may be selected from the group consisting of a chemokine receptor (e.g., CCR5, CCR3, CCR2b, and CXCR4) or anti-HIV chemokine antisera (polyclonal or monoclonal, or anti-peptide HIV chemokine antisera). In one illustration, the recombinant HIV chemokine or HIV chemokine may be purified from a culture of transfected or infected human cells. The cultured cells are lysed, cellular debris is removed by centrifugation, and the supernatant is then applied to an affinity column. The column is washed, and then the recombinant HIV chemokine or HIV chemokine is eluted from the immobilized affinity molecule using methods known in the art. The purified recombinant CXC or HIV chemokine preparation may then be checked for purity by sodium dodecyl sulfate polyacrylamide gel electrophoresis; and for activity by a binding assay. Alternatively, peptides derived from the HIV chemokine sequence can be linked to an affinity matrix (i.e. CNBr activated sepharose) and used to purify chemokine peptide-specific antibody for use in isolation and detection.

EXAMPLE 9

This embodiment illustrates that a monoclonal antibody (MAb) can be generated to epitopes specific for an HIV chemokine. Monoclonal antibodies to HIV chemokine may be developed using methods known in the art. For example, a method for making monoclonal antibodies immunoreactive with HIV chemokine involves the use of isolated and purified HIV chemokine as the immunogen; and an immunologically effective amount of the immunogen is used to immunize an animal (such as BALB/c mice) at timed intervals. A few days following the last immunization, spleens from the immunized animal are harvested aseptically, and placed into a tissue culture dish containing tissue culture medium. The primed spleen cells containing B-lymphocytes are mixed with a immunoglobulin non-secreting plasmacytoma cell line (usually a 10:1 to 1:1 ratio) for fusion. Fusion can be accomplished by methods including contacting the cells with a fusion agent such as polyethylene glycol (1 ml of a 50% solution, MW 1400) or by electrofusion. The cells from the fusion are then cloned out in microtiter plate wells. Typically, the plasmacytoma cell line is deficient in an enzyme such as hypoxanthine guanine phospho-ribosyl transferase such that fused hybridomas can be selected for by using a tissue culture selection medium such as a medium containing hypoxanthine, aminopterin, and thymidine. The hybridoma cultures are then incubated for several days, under standard tissue culture conditions, before the supernatants are tested for immunoreactivity to isolated and purified HIV chemokine. Alternatively, using methods standard in the art, human monoclonal antibodies may be made to an HIV chemokine (see. e.g., Ludwig et al, 1994, Cell. Imm.; Kanki and Takeuchi, 1995, Hum. Antibodies Hybridomas 6:89-92; Satoh et al., 1995, Immunol. Lett. 47:113-19; Vollmers et al., 1995, Cancer 76:550-558).

Murine monoclonals can be modified (making them more “human compatible”) for administration into an individual using techniques standard in the art (e.g., as reviewed by Adair, 1992, Immunological Reviews 130: 6-37, herein incorporated by reference). For example, murine monoclonal antibodies may be “humanized” by replacing portions of the murine monoclonal antibody with the equivalent human sequence. In one embodiment, a chlimeric antibody is constructed. The construction of chimeric antibodies is now a straightforward procedure (Adair, 1992, supra, at p. 13) in which the chimeric antibody is made by joining the murine variable region to a human constant region. Additionally, chimeric antibodies may be made by joining the hypervariable regions of the murine monoclonal antibody to human constant regions and parts of human variable regions using one of several techniques known in the art. Techniques for constructing chimeric antibodies (murine-human) of therapeutic potential have been described previously (see, e.g., Morrison et al., 1984, Proc. Natl. Acad. Sci. 81:6851-6855; Larrick et al., 1991, Hum. Antibod. Hybridomas 2:172-189; herein incorporated by reference). Thus, in one embodiment of the present invention, and using methods known in the art, the murine variable region of the monoclonal antibody to HIV chemokine according to the present invention is joined to a human constant region to form a chimeric anti-HIV chemokine monoclonal antibody having the same specificity as the anti-HIV chemokine MAb. In general, humanizing an murine MAb such as by making a chimeric antibody limits the development of human anti-mouse antibody responses. Additionally, the humanized antibodies generally change the pharmacokinetics by providing a longer half-life of such antibody, as compared to the half-life of murine antibody.

A chimeric MAb can also be constructed using a standard combination of techniques including polymerase chain reaction (PCR) cloning of antibody variable regions, the use of suitable expression vectors already containing the DNA encoding human constant region, insertion of the DNA for the murine MAb variable region into such vector in forming a recombinant vector, and expression of the resultant chimeric antibody by an expression system containing the recombinant vector (See, e.g., Daugherty et al., 1991, Nucl. Acids Res. 19:2471-2476; Maeda et al., 1991, Human Antibodies and Hybridomas 2:124-134; herein incorporated by reference). One expression vector can be used in which the vector is constructed so that the variable region and constant region genes are in tandem. Expression systems known to those skilled in the art for production of antibody or antibody fragments include mammalian cells (e.g. cell lines such as COS, NSO, or CHO), phage expression libraries, Escherichia coli, and yeast (Adair, 1992, supra). Any one of these monoclonal antibodies (purified human antibodies or purified, chimeric monoclonal antibodies) may then be tested for their ability to interact with HIV chemokine in binding assays.

Anti-HIV chemokine antibodies may also be used in competitive drug screening assays to identify compounds that function to bind HIV chemokine thereby neutralizing one or more functional activities of HIV chemokine (e.g., chemotaxis, and/or chemokine receptor binding). For example, a drug compound is tested for its ability to compete with neutralizing antibodies (capable of binding HIV chemokine) for binding to HIV chemokine. Selection of such possible drug compounds may also be facilitated by methods known in the art including determination of the three-dimensional structure of HIV chemokine (e.g., x-ray crystallography and/or computer modeling).

EXAMPLE 10

This Example illustrates the use of HIV chemokine or antibodies to HIV chemokine for use in diagnostic assays. HIV chemokine, isolated according to the method of the present invention, or peptides formed therefrom, can be used as an antigen for diagnostic assays. Alternatively, HIV chemokine, or peptides formed therefrom, can be used as immunogens for generating anti-HIV chemokine antisera of diagnostic value. Antigenic sires of a protein may vary in size but can consist of from about 7 to about 14 amino acids. Thus, a protein the size of HIV chemokine may contain several discrete antigenic epitopes. Using synthetic processes, peptides of at least 7 to 14 amino acids in size may be generated which contain antigenic epitopes of HIV chemokine. The peptides can be synthesized from the amino acid sequence of an HIV chemokine using one of the several methods of peptide synthesis known in the art including standard solid peptide synthesis using tertbutyl-oxycarbonyl amino acids (Mitchell et al., 1978, J. Org. Chem. 43:2845-2852); using 9-fluorenylmethyloxycarbonyl amino acids on a polyamide support (Dryland et al., 1986, J. Chem. So. Perkin Trans. I, 125-137); by pepscan synthesis (Geysen et al., 1987, J. Immunol. Methods 03:259; 1984, Proc. Natl. Acad. Sci. USA 81:3998); or by standard liquid phase peptide synthesis. Modification of the peptides, such as by deletion and substitution of amino acids (and including extensions and additions to amino acids) and in other ways, may be made so as to not substantially detract from the immunological properties of the peptide. In particular, the amino acid sequence of the peptide may be altered by replacing one or more amino acids with functionally equivalent amino acids resulting in an alteration which is silent in terms of an observed differences in the binding specificity of the peptide.

In one embodiment, purified HIV chemokine, or peptides formed therefrom, may be used as antigens in immunoassays for the detection of antisera present in the body fluid of an individual. The body fluids include, but are not limited to, blood (e.g., serum) and urine. A diagnostic assay utilizing as an antigen HIV chemokine or a peptide formed therefrom, includes any immunoassay known in the art including, but not limited to, radioimmunoassay, ELISA, “sandwich” assay, precipitin reaction, agglutination assay, fluorescent immunoassay, and chemiluminescence-based immunoassay. Thus, for example, HIV chemokine or a peptide formed therefrom may be used as an antigen in an ELISA in which the antigen is immobilized to a selected surface; followed by blocking of unbound areas of the surface; contacting the body fluid sample with the selected surface containing immobilized antigen; washing the surface to remove materials in the sample which are not bound to the antigen; and detection of any immune complexes present (e.g., antibody to HIV chemokine complexed to the antigen) with a detectable moiety, such as by adding protein A peroxidase with subsequent color development. Other detectable moieties, conjugates and/or substrates known to those skilled in the art of diagnostics may be used to detect immunocomplexes formed. Thus, a diagnostic kit may contain the isolated HIV chemokine, or peptide formed therefrom as the antigen; a means for facilitating contact between the sample to be analyzed and the antigen (e.g., for an ELISA, a microtiter plate or wells); and a means for detecting the presence of immunocomplexes formed.

In another embodiment of the invention, using antisera to epitopes of an HIV chemokine, the clinical sample is assayed for the presence of the antigen, i.e., HIV chemokine. This antisera may be used by contacting the clinical sample, and detecting the presence of immunocomplexes formed between the antisera and antigen that is present in the clinical sample. Thus, a diagnostic kit may contain the antibody generated to HIV chemokine epitopes; a means for facilitating contact between the clinical sample and the antibody; and a means for detecting the presence of immunocomplexes formed.

EXAMPLE 11

This embodiment of the present invention is to provide HIV chemokines, peptides formed therefrom, or modified variant of HIV chemokines (separately or collectively referred to as “HIV chemokine immunogen”) to be used as immunogens in a prophylactic and/or therapeutic vaccine for active immunization to protect against or treat infections caused by HIV. For vaccine development, an HIV chemokine comprising the immunogen may be purified from HIV infected cells, or comprise recombinant HIV chemokine, using the methods according to the present invention. The HIV chemokine immunogen is included as the relevant immunogenic material in the vaccine formulation, and in immunoeffective amounts, to induce an immune response. Many methods are known for the introduction of a vaccine formulation into the human to be vaccinated. These include, but are not limited to, intradermal, intramuscular, intraperitoneal, intravenous, subcutaneous, ocular, intranasal, and oral administration. As known to those skilled in the art, the vaccine may further comprise a physiological carrier such as a pharmaceutically acceptable solution, polymer or liposomes; and an adjuvant, or a combination thereof.

Various adjuvants are used in conjunction with vaccine formulations. The adjuvants aid in attaining a more durable and higher level of immunity using smaller amounts of vaccine antigen or fewer doses than if the vaccine antigen were administered alone. The adjuvant may act to stimulate the immune effector cells, as well as delay release and degradation/processing of the HIV chemokine immunogen to enhance immune recognition. Examples of adjuvants include incomplete Freund's adjuvant, Adjuvant 65 (containing peanut oil, mannide monooleate and aluminum monostearate), oil emulsions, glycolipid analogs, lipopeptides, Ribi adjuvant, the pluronic polyols, polyamines, Avridine, Quil A, saponin, MPL, QS-21, and mineral gels such as aluminum hydroxide, aluminum phosphate, etc.

Another embodiment of this mode of the invention involves peptides derived from HIV chemokine as a hapten, i.e. a molecule which cannot by itself elicit an immune response. In such case, the hapten may be covalently bound to a carrier or other immunogenic molecule which will confer immunogenicity to the coupled hapten when exposed to the immune system. Thus, such an HIV chemokine-specific hapten liked to a carrier molecule may be the immunogen in a vaccine formulation. There are many such carriers known in the art including, but not limited to, keyhole limpet hemocyanin, bovine serum albumin, and diphtheria toxin cross-reactive mutant protein (“CRM”). Additionally, there are several methods known in the art for conjugating a peptide to a carrier. Such methods include, but are not limited to, the use of glutaraldehyde, or succinimidyl m-maleimidobenzoate, or 1-ethyl-3-(3-dimethyl-aminopropyl)carbodiimide, or the use of bromo-acetylated peptide (see, e.g. Robey et al., 1989, Anal. Biochem. 177:373-377).

In another embodiment, as an alternative to active immunization, such as where an individual is suffering from late stages of AIDS, immunization may be passive, i.e. immunization comprising administration of a therapeutically effective amount of purified human-compatible anti-HIV chemokine antibodies (e.g., chimeric or human compatible monoclonal antibodies).

EXAMPLE 12

This Example illustrates methods of administration of HIV chemokine, peptides formed therefrom, or modified variant of HIV chemokine, as agonists or antagonists (separately or collectively referred to as “HIV chemokine therapeutic”). The HIV chemokine therapeutic may be formulated in a pharmaceutically acceptable, nontoxic, carrier. Pharmaceutically acceptable carriers are generally known to include aqueous solutions such as water, various phosphate buffers, various buffered salines, alcoholic/aqueous solutions, and emulsions or suspensions; wherein the ionic strength, pH, and other properties of the pharmaceutically acceptable carrier may be adjusted to maximize delivery and activity of the HIV chemokine therapeutic to that site. Regarding pH, generally a pH range of 6 to 8 is typically used. It will be appreciated by those skilled in the art that the carrier may comprise any suitable pharmaceutically acceptable liposome having incorporated therein an HIV chemokine therapeutic according to the present invention. Such liposomal compositions may be administered in any conventional mode for therapeutic treatment. The pharmaceutically acceptable carrier may additionally comprise an agent that may improve the solubility of the HIV chemokine therapeutic while not inhibiting the binding activity of the HIV chemokine therapeutic. Such an additional agent may include, but is not limited to, a low concentration (e.g. concentration of 0.1% or less) of a nonionic detergent.

Depending on the physiologic site to be treated, the health of the individual to be treated, and the nature of the formulation, the HIV chemokine therapeutic may be administered in any one of the standard methods known in the art for administration of therapeutic agents, including, but not limited to, topical, by injection (e.g., intravenously), aerosol spray, intranasal, transmucosal, transdermal, and orally (by administered pills or liquids). As appreciated by those skilled in the art, dosage and frequency of dosage of an HIV chemokine therapeutic will depend on multiple patient variables, including the severity of AIDS, age, weight, responsiveness to therapy, tolerance of therapeutic, and clearance rate of therapeutic.

Having described the preferred embodiments of the present invention, it will be apparent to one of ordinary skill in the art that various modifications may be made to the disclosed embodiments, and that such modifications are intended to be within the scope of the present invention.

26 1 540 DNA Human immunodeficiency virus dsDNA intermediate of lbl revINRold (Note antisense gene of negative polarity with respect to HIV-1 usual coding region) 1 aggcaagctt tattgaggct taagcagtgg gttccctagt 40 tagccagaga gctcccaggc tcagatctgg tctaaccaga 80 gagacccagt acaggcaaaa agcagctgct tatatgtagc 120 atctgagggc tcgccactcc ccagtcccgc ccaggccaca 160 cctccctgga aagtccccag cggaaagtcc cttgtagaaa 200 gctcg atg tca gca gtc ttt gta gta ctc cgg atg 235 cag ctc tcg ggc cat gtg acg aaa tgc t agg agg 269 ctg tca aac ttc cac act aat act tct ccc tcc 302 ggg tcc tcc atc cca tgc tgg ctc ata ggg tgt 335 aac aag ctg ttc ttc tct cct tat ttg gcc tct 368 tct act tgc tct ggt tca act ggt act aac ttg 401 aag cac cat cca aag gtc agt gga tat ctg atc 434 cct ggc cct ggt gtg tag ttctgccaat 462 cagggaagta gccttgtgtg tggtagatcc acagatcaag 502 gatctcttgt cttttttggg accaaattag cccttcca 540 2 81 PRT Human immunodeficiency virus HIV chemokine protein from lbl revINRold 2 Met Ser Ala Val Phe Val Val Leu Arg Met Gln Leu 5 10 Ser Gly His Val Thr Lys Cys Arg Arg Leu Ser Asn 15 20 Phe His Thr Asn Thr Ser Pro Ser Gly Ser Ser Ile 25 30 35 Pro Cys Trp Leu Ile Gly Cys Asn Lys Leu Phe Phe 40 45 Ser Pro Tyr Leu Ala Ser Ser Thr Cys Ser Gly Ser 50 55 60 Thr Gly Thr Asn Leu Lys His His Pro Leu Val Ser 65 70 Gly Tyr Leu Ile Pro Gly Pro Gly Val 75 80 3 22 DNA Human immunodeficiency virus 5′ sense primer 3 tttcgtcaca tggcccgagc gc 22 4 25 DNA Human immunodeficiency virus 3′ antisense primer 4 ccagagagac ccagtacagg caaaa 25 5 20 DNA human immunodeficiency virus 3′ MaeI antisense primer 5 ttccctagtt agccagagag 20 6 390 RNA Human immunodeficiency virus antisense RNA originating off HIVaINR in SF2 HIV strain 6 agaucugguc uaaccagaga gacccaguac aggcaaaaag 40 cagcugcuua uaugcagcau cugagggcac gccacucccc 80 agucccgccc aggccacgcc ucccuggaaa guccccagcg 120 gaaagucccu uguagaaagc ucgaugucag cagucuuugu 160 aguacuccgg augcagcucu cgggccaugu gaugaaaugc 200 uaguuugcug ucaaaccucc acacuaacac uucuuucucc 240 gcguccucca ucccaugcag gcucauaggg uguaacaagc 280 uguuguucuc uccuucauug gccucuucua ccuucucugg 320 cucaacuggu acuagcuuga agcaccaucc aaaggucagu 360 ggauaucuga ucccuggccc ugguguguag 390 7 112 PRT Human immunodeficiency virus HIV chemokine protein (1st start site;(+1) ribosomal frameshift at nucleotide 133; and (-1) ribosomal shift at nucleotide 265) from SF2 HIV 7 Met Gln His Leu Arg Ala Arg His Ser Pro Val Pro 5 10 Pro Arg Pro Arg Leu Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Arg Lys Leu Asp Val Ser Ser Leu Cys 25 30 35 Ser Thr Pro Asp Ala Ala Leu Gly Pro Cys Asp Glu 40 45 Met Leu Val Cys Cys Gln Thr Ser Thr Leu Thr Leu 50 55 60 Leu Ser Pro Arg Pro Pro Ser His Ala Gly Ser Ile 65 70 Gly Cys Asn Lys Leu Leu Phe Ser Pro Ser Leu Ala 75 80 Ser Ser Thr Phe Ser Gly Ser Thr Gly Thr Ser Leu 85 90 95 Lys His His Pro Lys Val Ser Gly Tyr Leu Ile Pro 100 105 Gly Pro Gly Val 110 8 82 PRT Human immunodeficiency virus HIV chemokine protein (2nd start site; (-1) ribosomal shifts at nucleotides 200 and 265)from SF2 HIV 8 Met Ser Ala Val Phe Val Val Leu Arg Met Gln Leu 5 10 Ser Gly His Val Met Lys Cys Leu Val Cys Cys Gln 15 20 Thr Ser Thr Leu Thr Leu Leu Ser Pro Arg Pro Pro 25 30 35 Ser His Ala Gly Ser Ile Gly Cys Asn Lys Leu Leu 40 45 Phe Ser Pro Ser Leu Ala Ser Ser Thr Phe Ser Gly 50 55 60 Ser Thr Gly Thr Ser Leu Lys His His Pro Lys Val 65 70 Ser Gly Tyr Leu Ile Pro Gly Pro Gly Val 75 80 9 81 PRT Human immunodeficiency virus HIV chemokine protein (2nd start site; (+1) ribosomal shift at nucleotide 201)from SF2 HIV 9 Met Ser Ala Val Phe Val Val Leu Arg Met Gln Leu 5 10 Ser Gly His Val Met Lys Cys Ser Leu Leu Ser Asn 15 20 Leu His Thr Asn Thr Ser Phe Ser Ala Ser Ser Ile 25 30 35 Pro Cys Arg Leu Ile Gly Cys Asn Lys Leu Leu Phe 40 45 Ser Pro Ser Leu Ala Ser Ser Thr Phe Ser Gly Ser 50 55 60 Thr Gly Thr Ser Leu Lys His His Pro Lys Val Ser 65 70 Gly Tyr Leu Ile Pro Gly Pro Gly Val 75 80 10 112 PRT Human immunodeficiency virus HIV chemokine protein (1st start site at nucleotide 52; (+1) ribosomal frameshift at nucleotide 133, (-1) ribosomal frameshift at nucleotide 265) from (Pt)CNS HIV 10 Met Gln His Leu Arg Ala Arg His Ser Pro Val Pro 5 10 Pro Arg Pro His Leu Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Arg Lys Phe Asp Val Ile Ser Ser Cys 25 30 35 Ser Thr Pro Asp Ala Ala Leu Gly Pro Cys Gly Glu 40 45 Met Leu Gly Cys Cys Gln Thr Ser Thr Leu Thr Leu 50 55 60 Leu Ser Pro Gly Arg Pro Ser His Ala Gly Ser Ile 65 70 Gly Cys Asn Ser Thr Leu Phe Ser Pro Ser leu Ala 75 80 Ser Ser Ile Phe Ser Gly Ser Thr Gly Thr Ser Leu 85 90 95 Lys His His Pro Lys Val Ser Gly Tyr Leu Val Pro 100 105 Gly Pro Gly Val 110 11 112 PRT Human immunodeficiency virus HIV chemokine protein (1st start site; (-1) ribosomal frameshift at nucleotide 133, (+1) ribosomal frameshift at 265), from (Pt)CNS HIV 11 Met Gln His Leu Arg Ala Arg His Ser Pro Val Pro 5 10 Pro Arg Pro His Leu Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Val Glu Ser Ser Met Ser Ser Val Leu 25 30 35 Val Val Leu Arg Met Gln Leu Ser Gly Pro Val Val 40 45 Lys Cys Arg Val Lys Ser Asn Phe His Thr Asn Thr 50 55 60 Ser Leu Ser Gly Ser Ser Ile Pro Cys Arg Leu Ile 65 70 Gly Cys Asn Asn Thr Leu Phe Ser Pro Ser Leu Ala 75 80 Ser Ser Ile Phe Ser Gly Ser Thr Gly Thr Ser Leu 85 90 95 Lys His His Pro Lys Val Ser Gly Tyr Leu Val Pro 100 105 Gly Pro Gly Val 110 12 117 PRT Human immunodeficiency virus HIV chemokine protein (1st start site; (+1) ribosomal frameshift at nucleotide 133, (-1) ribosomal frameshift at nucleotide 280) from (Pt)LN/SP HIV 12 Met Gln His Leu Arg Ala Arg His Ser Pro Val Pro 5 10 Pro Ser Pro Arg Leu Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Arg Lys Leu Gly Val Ser Ser Gly Gly 25 30 35 Val Ser Ser Ser Cys Ser Ser Pro Asp Ala Ala Leu 40 45 Gly Leu Arg Asp Glu Met Pro Gly Gly Cys Gln Thr 50 55 60 Ser Thr Leu Arg Leu Leu Ser Lys Gly Arg Pro Ser 65 70 His Ala Gly Ser Ile Gly Cys Asn Arg Leu Leu Phe 75 80 Ser Pro Ser Leu Ala Ser Ser Ile Phe Ser Ala Ser 85 90 95 Thr Gly Thr Ser Leu Lys His His Pro Lys Val Ser 100 105 Gly Tyr Leu Ile Pro Gly Pro Gly Val 110 115 13 118 PRT Human immunodeficiency virus HIV chemokine protein (1st start site; (-1) ribosomal frameshift at nucleotide 133, (+1) ribosomal frameshift at nucleotide 280) from (Pt)LN/SP HIV 13 Met Gln His Leu Arg Ala Arg His Ser Pro Val Pro 5 10 Pro Ser Pro Arg Leu Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Val Glu Ser Ser Val Ser Ala Val Ser 25 30 35 Met Ser Ala Val Leu Val Val Val Arg Met Gln Leu 40 45 Ser Gly Tyr Val Met Lys Cys Gln Ala Ala Val Lys 50 55 60 Pro Pro Leu Leu Arg Leu Leu Ser Leu Gly Pro Pro 65 70 Ser His Ala Gly Ser Ile Gly Cys Asn Arg Leu Leu 75 80 Phe Ser Pro Ser Leu Ala Ser Ser Thr Phe Ser Ala 85 90 95 Ser Thr Gly Thr Ser Leu Lys His His Pro Lys Val 100 105 Ser Gly Tyr Leu Ile Pro Gly Pro Gly Val 110 115 14 112 PRT Human immunodeficiency virus HIV chemokine protein (1st start site; (-1) ribosomal frameshift at nucleotide 133, (+1) ribosomal frameshift at nucleotide 265) from SF2 HIV 14 Met Gln His Leu Arg Ala Arg His Ser Pro Val Pro 5 10 Pro Arg Pro Arg Leu Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Val Glu Ser Ser Met Ser Ala Val Phe 25 30 35 Val Val Leu Arg Met Gln Leu Ser Gly His Val Met 40 45 Lys Cys Ser Leu Leu Ser Asn Leu His Thr Asn Thr 50 55 60 Ser Phe Ser Ala Ser Ser Ile Pro Cys Arg Leu Ile 65 70 Gly Cys Asn Lys Leu Leu Phe Ser Pro Ser Leu Ala 75 80 Ser Ser Thr Phe Ser Gly Ser Thr Gly Thr Ser Leu 85 90 95 Lys His His Pro Lys Val Ser Gly Tyr Leu Ile Pro 100 105 Gly Pro Gly Val 110 15 112 PRT Human immunodeficiency virus Xaa is any amino acid 28,37,47 HIV chemokine protein with read-through from SF2 HIV 15 Met Gln His Leu Arg Ala Arg His Ser Pro Val Pro 5 10 Pro Arg Pro Arg Leu Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Xaa Lys Ala Arg Cys Gln Gln Ser Leu 25 30 35 Xaa Tyr Ser Gly Cys Ser Ser Arg Ala Met Xaa Ser 40 45 Asn Ala Ser Leu Leu Ser Asn Leu His Thr Asn Thr 50 55 60 Ser Phe Ser Ala Ser Ser Ile Pro Cys Arg Leu Ile 65 70 Gly Lys Asn Lys Leu Leu Phe Ser Pro Ser Leu Ala 75 80 Ser Ser Thr Phe Ser Gly Ser Thr Gly Thr Ser Leu 84 90 95 Lys His His Pro Lys Val Ser Gly Tyr Leu Ile Pro 100 105 Gly Pro Gly Val 110 16 111 PRT Human immunodeficiency virus HIV chemokine protein from YU2 strain with a (+1) and (-1) ribosomal frameshift 16 Met Gln His Leu Arg Ala Arg His Ser Pro Val Pro 5 10 Pro Arg Pro Arg Phe Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Arg Lys Leu Glu Val Ile Ser Ser Cys 25 30 35 Ser Thr Pro Asp Ala Ala Leu Gly Pro Arg Asp Glu 40 45 Met Leu Val Cys Cys Gln Thr Ser Thr Leu Thr Leu 50 55 60 Leu Ser Pro Gly His Pro Phe His Ala Gly Ser Ile 65 70 Gly Cys Asn Lys Gln Leu Phe Ser Pro Ala Leu Ala 75 80 Ser Ser Ile Phe Ser Gly Ser Thr Gly Thr Ser Leu 85 90 95 Lys His His Pro Lys Val Ser Gly His Leu Val Pro 100 105 Pro Gly Val 110 17 111 PRT Human immunodeficiency virus HIV chemokine protein (1st start site; (-1) ribosomal frameshift at nucleotide 133, (+1) ribosomal frameshift at nucleotide 265) from YU2 HIV 17 Met Gln His Leu Arg Ala Arg His Ser Pro Val Pro 5 10 Pro Arg Pro Arg Phe Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Val Glu Ser Ser Arg Ser Ser Val Leu 25 30 35 Val Val Leu Arg Met Gln Leu Ser Gly His Val Met 40 45 Lys Cys Arg Arg Leu Ser Asn Leu His Ser Asn Pro 50 55 60 Ser Leu Ser Gly Ser Ser Ile Pro Cys Trp Leu Ile 65 70 Gly Cys Asn Lys Gln Leu Phe Ser Pro Ala Leu Ala 75 80 Ser Ser Ile Phe Ser Gly Ser Thr Gly Thr Ser Leu 85 90 95 Lys His His Pro Lys Val Ser Gly His Leu Val Pro 100 105 Pro Gly Val 110 18 111 PRT Human immunodeficiency virus Xaa is any amino acid 28,37,47 HIV chemokine protein with read-through from YU2 HIV 18 Met Gln His Leu Arg Ala Arg His Ser Pro Val Pro 5 10 Pro Arg Pro Arg Phe Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Xaa Lys Ala Arg Gly His Gln Phe Leu 25 30 35 Xaa Tyr Ser Gly Cys Ser Ser Arg Ala Thr Xaa Ser 40 45 Asn Ala Arg Arg Leu Ser Asn Leu His Ser Asn Pro 50 55 60 Ser Leu Ser Ala Ser Ser Ile Pro Cys Trp Leu Ile 65 70 Gly Cys Asn Lys Gln Leu Phe Ser Pro Ala Leu Ala 75 80 Ser Ser Ile Phe Ser Gly Ser Thr Gly Thr Ser Leu 85 90 95 Lys His His Pro Lys Val Ser Gly His Leu Val Pro 100 105 Pro Gly Val 110 19 112 PRT Human immunodeficiency virus 28,37,97 Xaa is any amino acid HIV chemokine protein with read-through from ELI strain of HIV 19 Met Gln His Leu Arg Val Ser His Ser Pro Val Pro 5 10 Pro Ser Pro Arg Leu Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Xaa Lys Ala Arg Cys His Gln Phe Leu 25 30 35 Xaa Asn Ser Gly Cys Ile Ser Arg Ala Leu Cys Ser 40 45 Asn Ala Ser Leu Leu Leu Asn Leu His Phe Asn Thr 50 55 60 Cys Leu Ser Gly Ser Ser Ile Pro Cys Trp His Ile 65 70 Gly Cys Asn Lys Leu Leu Val Ser Pro Ser Val Ser 75 80 Ser Ser Thr Ser Cys Gly Ser Thr Gly Thr Ser Ser 85 90 95 Xaa His His Pro Lys Val Ser Gly Tyr Leu Ile Pro 100 105 Gly Pro Gly Val 110 20 106 PRT Human immunodeficiency virus Xaa is any amino acid 28,38,73 HIV chemokine protein with read-through from dual-tropic strain p896 of HIV 20 Met Gln His Leu Arg Ala Arg His Ser Pro Val Arg 5 10 Pro Arg Pro his Leu Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Xaa Ile Ala Gln Cys Gln Gln Phe Ser 25 30 35 Ser Xaa Ser Thr Pro Asp Ala Ala Leu Gly Pro Arg 40 45 Asp Gly Met Leu Gly Gly Cys Gln Thr Ser thr Leu 50 55 60 Thr Leu Val Ser Pro Ser Leu Leu Leu His Ala Gly 65 70 Xaa Gln Gly Val Ala Ser Cys Cys Pro Leu Cys Cys 75 80 Ser Leu Leu His Leu Ala Gln Leu Val Leu Ala Cys 85 90 95 Ser Thr Ile Gln Arg Ser Val Ile Asp Ile 100 105 21 443 RNA Human immunodeficiency virus antisense RNA sequence from pHIVCAT 21 agaucugguc uaaccagaga gacccaguac aggcaaaaag 40 cagcugcuua uaugcagcau cugagggcuc gccacucccc 80 agucccgccc aggccacgcc ucccuggaaa guccccagcg 120 gaaagucccu uguaacaagc ucgaugucaa caguucuuga 160 aguacuccgg augcagcucu cgggccacgu gaugaaaugc 200 uaggcggcug ucaaaccucc acucuaacac uucucucuca 240 gggucaucca uuccaugcag gcucacaggg uguaacaagc 280 ugguguucuc uccuuuauug gccucuucua ccuuaucugg 320 cucaacuggu acuagcuugu agcaccaucc aaaggucagu 360 ggauaucuga cuccuggccc ugguguguag uucugcuaau 400 cagggaagua gccuugugug ugguagaucc acagaucaag 440 gau 443 22 46 PRT Human immunodeficiency virus Xaa is any amino acid 28 HIV chemokine protein with read-through at nucleotides 133-135 from pHIVCAT 22 Met Gln His Leu Arg Ala Arg His Ser Pro Val Pro 5 10 Pro Arg Pro Arg Leu Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Xaa Gln Ala Arg Cys Gln Gln Phe Leu 25 30 35 Lys Tyr Ser Gly Cys Ser Ser Arg Ala Thr 40 45 23 35 PRT Human immunodeficiency virus HIV chemokine protein with (+1) frameshift at nucleotide 134 from pHIVCAT 23 Met Gln His Leu Arg Ala Arg His Ser Pro Val Pro 5 10 Pro Arg Pro Arg Leu Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Asn Lys Leu Asp Val Asn Ser Ser 25 30 35 24 112 PRT Human immunodeficiency virus Xaa is any amino acid 97 HIV chemokine protein with (-1) frameshift at nucleotide 133, (+1) frameshift at nucleotide 205, readthrough at nucleotides 341-343 from pHIVCAT 24 Met Gln His Leu Arg Ala Arg His Ser Pro Val Pro 5 10 Pro Arg Pro Arg Leu Pro Gly Lys Ser Pro Ala Glu 15 20 Ser Pro Leu Val Thr Ser Trp Met Ser Thr Val Leu 25 30 35 Glu Val Leu Arg Met Gln Leu Ser Gly His Val Met 40 45 Lys Cys Arg Arg Leu Ser Asn Leu His Ser Asn Thr 50 55 60 Ser Leu Ser Gly Ser Ser Ile Pro Cys Arg Leu Thr 65 70 Gly Cys Asn Lys Leu Val Phe Cys Pro Leu Leu Ala 75 80 Ser Ser Thr Leu Ser Gly Ser Thr Gly Thr Ser Leu 85 90 95 Xaa His His Pro Lys Val Ser Gly Tyr Leu Thr Pro 100 105 Gly Pro Gly Val 110 25 419 RNA Human immunodeficiency virus antisense RNA sequence from an HIV from the CNS of a patient 25 agaucugguc uaacaagaga gacccaguac aagcgaaaag 40 cagcugcuua uaugcagcau cugagggcac gccacucccg 80 agucccgccc aggccacycc ucccuggaaa guccccagcg 120 gaaagucccu uguagaaagu ucgaugucau caguucuugu 160 aguacuccgg augcagcucu cgggcccugu ggugaaaugc 200 uagggugcug ucaaaucucc acacuaacac uucucucucc 240 gggugcucca ucccaugcag gcacauaggg uguaagauac 280 uguuguucuc uccuucauug ccuucuucua ucuucucugc 320 ucaacuggua cuagcugaaa gcaccaucca aaggucagug 360 gauaucugau cccuggcccu gguguguagu ugugccaauc 400 agggaaguag ccuugugug 419 26 419 RNA Human immunodeficiency virus antisense RNA sequence from an HIV from the lymph node and spleen of a patient 26 agaucugguc uaacuagaga gacccaguac aggcaaagag 40 cagcugcuua uaugcagcau cugagggcac gccacucccg 80 agucccgccc aguccacycc ucccuggaaa guccccagcg 120 gaaagucccu uguagaaagu ucgaugucau caguucuugu 160 aguaguccgg augcagcucu cgggcuacgu ggugaaaugc 200 caggcggcug ucaaaucucc acucuaagac uucucucucc 240 ggguccucca ucccaugcag gcacauagga uguaagaggc 280 uguuguucuc uccuucauug gcuucuucua cuuucucucc 320 ucaacuggua cuagcuuaaa gcaccaucca aaggucagug 360 gauaucugau cccuggcccu gguguguagu ucugccaauc 400 agggaaguag ccuugugug 419 

What is claimed is:
 1. An isolated polynucleotide encoding a HIV protein having a sequence selected from the group consisting of SEQ ID NO:7; SEQ ID NO:8 and SEQ ID NO:9.
 2. The isolated polynucleotide of claim 1, wherein the protein has a sequence of SEQ ID NO:7.
 3. The isolated polynucleotide of claim 1, wherein the protein has a sequence of SEQ ID NO:8.
 4. The isolated polynucleotide of claim 1, wherein the protein has a sequence of SEQ fD NO:9.
 5. The isolated polynucleotide of claim 1, wherein the polynucleotide is RNA.
 6. The isolated polynucleotide of claim 1, wherein the polynucleotide is DNA.
 7. An isolated nucleic acid molecule having a sequence of SEQ ED NO:6. 